James R. Rosowski

VALVE AND BAND MORPHOLOGY OF SOME FRESHWATER DIATOMS. II. INTEGRATION OF VALVES AND BANDS IN NAVICULA CONFERVACEA VAR. CONFERVACEA12

Chemically cleaned and critical‐point dried cells of a clonal culture were examined with scanning electron microscopy. Cells form filaments by valve‐to‐valve connections maintained by organic material which adheres to the central area of the valve face. Bending of filaments is probably restricted to some extent by the articulation of overlapping spatulate marginal spines with an adjacent underlapping set of much shorter spines (ridges), and with the mantle edge itself. Cell division results in three possible spine patterns for each cell: a set of overlapping and a set of underlapping spines; no overlapping sets of spines (two underlapping); or two sets of overlapping spines (no underlapping). Each filament inherits cells with spine set patterns in the ratio of 2 (with 1 set overlapping): 1 (with no sets overlapping): 1 (with 2 sets overlapping). Valvocopulae are shaped similarly to pleurae except that the partes exteriores of the valvocopulae are wider. The pars interior of both is delimited by an advalvar row of pores continuous around the cell apex. The pars exterior also has a row of pores, but it is median in the valvocopula and first pleura and does not continue around the cell apex. The valvocopulae always underlap the mantle and the pleurae always underlap their preceding band. The ends of both appeared attached, but may become free in acid‐cleaned preparations. Bands alternate with each other so that the ends of the valvocopula attach to the first continuous apical portion of the first pleura; the ends of the first pleura attach in that same fashion to the second pleura but at the opposite apex; and all subsequent pleurae alternate in the same fashion with up to at least 13 pleurae/epicingulum. The continuous apical portion of each band is elevated so that a functional (but not structural) ligula is formed, with the continuous apical portion of alternate bands becoming adjacent and underlapping each other only in this region. The valvocopulae in a single cell, or of adjacent cells, may have their continuous apical ends on the same or on opposite apices. It is recommended that N. confervacea var. peregrina (W. Sm.) Grun. be merged with the nominate variety.

TRACHELOMONAS HISPIDA VAR. CORONATA (EUGLENOPHYCEAE). I. ULTRASTRUCTURE OF CYTOSKELETAL AND FLAGELLAR SYSTEMS1,2

Trachelomonas hispida var. coronata Lemm. has a fibrous, mucilaginous, ovoid, mineralized envelope (lorica), the ornamentation and coloration of which are capricious in culture. Cells exhibit a radial distribution of most organelles: (i) A cortical endoplasmic reticulum, (ii) parietal chloroplasts, and (iii) a median vacuolar region surrounded by several Golgi bodies and diverse vesicles. Associated with the emergent flagellum is a “paraflagellar complex” that consists of dense globules, cross‐striated ribbon‐like structures, a paraflagellar body, and an array of parallel striated filaments. The stigma consists of a single layer of pigmented granules that partially surrounds the canal/reservoir transition zone where microtubular bands intersect. A microtubular cytoskeleton consists of pellicular microtubules, peri‐canal microtubules, stigma‐associated microtubules and para‐reservoir microtubules. The thickenings on the posterior, concave margins of the pellicular strips suggest that this pellicle is of intermediate complexity between those of Euglena spirogyra (Ehrenb. and Trachelomonas volvocina (Ehrenb.).

VALVE AND BAND MORPHOLOGY OF SOME FRESHWATER DIATOMS. III. PRE‐ AND POST‐AUXOSPORE FRUSTULES AND THE INITIAL CELL OF MELOSIRA ROESEANA1

Frustules of a clonal culture of Melosira roeseana Rabenh. were examined with light and scanning electron microscopy. Vegetative valves in the post‐auxospore (full size) stage exhibit a larger width/length ratio than those in the pre‐auxospore (size‐reduced) stage. Cells form chains by linking spines of adjacent valves which occur at the periphery of the valve face‐mantle junction. Three or jour large pores occur at the center of the valve face, with the diameter of each pore tapering from the inner to the outer valve surface; these pores are often occluded by siliceous processes. Features of M. roeseana, not shown previously for Melosira, include a “stepped” mantle, on only one of the two valves resulting from the same cell division, flattened processes attached to short siliceous stalks on the valve face, disk‐like processes on the mantle, and an open girdle band with up to eight antiligulae. Siliceous scales on the surface of the initial cell are remnants of the auxospore wall. The epivalve of the initial cell is larger in diameter than the hypovalve, and both valves lack linking spines and a step on the valve surface. The initial, cell epicingulum consists of only two bands; the hypocingulum has up to seven. Initial cells with four or more hypocingular bands divide to form new post‐auxospore filaments. Melosira roeseana should not be included in the genus Melosira as it is presently defined by the type species, M. nurnmuloides C. Ag. Major differences include irregular linking spines, a closed pseudoloculate valve construction, and labiate processes on the valve face and mantle of M. nummuloides, compared with well‐defined linking spines, a valve constructed of a basal siliceous layer perforated by poroid areolae, and labiate processes lacking on the valve of M. roeseana.

VALVE AND BAND MORPHOLOGY OF SOME FRESHWATER DIATOMS I. FRAGILARIA CAPUCINA VAR. MESOLEPTA1,2

Acid cleaned cells from clonal cultures of Fragilaria capucina var. mesolepta Rabh. were examined with light and scanning electron microscopy. Recently isolated cells are linear‐lanceolate in shape with a median constriction. After several transfers over 25 mo, cells exhibit size diminution resulting in small elliptically shaped valves. Adjacent valves are united to one another by interlocking marginal spines. Every valve has an apical pore field at each apex. A single labiate process is present infrequtently, appearing underdeveloped most often in size‐reduced cells. The girdle region consists of two cingula, each composed of a series of underlapping bands. Each pleura in the series is a discontinuous ring with a central ligula. A survey of past ultrastructure studies on the freshwater Fragilariaceae reveals that the occurrence of the apical pore field and labiate process are likely key characteristics for the family. The apical pore field of Diatoma, Asterionella and Tabellaria is positioned on the valve face, whereas the apical pore field of F. capucina var. mesolepta is located on the valve mantle, the girdle region of F. capucina var. mesolepta is basically similar to that of Gomphonema parvulum (Kütz.) Grun.

EXTRACELLULAR ASSOCIATION AND ADAPTIVE SIGNIFICANCE OF THE BAS-RELIEF MUCILAGE PAD OF ACHNANTHES LANCEOLATA (BACILLARIOPHYCEAE)

Glass microscope slides were immersed in the tiny Headwaters of a midwestern stream Achnanthes lanceolata (Breb.) Grunow was the dominant or co-dominant species in 14 out of 15 one-month-old communities over a two-year period. Minutely streaked, periphyton-free areas mostly lacked live diatoms but had cell-free mucilage pads and attached raphe valves of A. lanceolata. These pads, secure or peeling, had a distinct bas-relief impression of the raphe valve. Pad mucilage was associated with the puncta and raphe, and its presence in the puncta of raphe valves maximizes the surface for valve/substrate adhesion. Periphyton-free streaks in otherwise stable periphyton may represent areas where abrasion or grazing had killed or removed cells without dislodging the mucilage-secured raphe valves or valve-free mucilage pads. Important adaptive features of A. lanceolata for resisting graying and/or stream hydrodynamic forces appear to be: a sessile, low-profile, lanceolate life form with rounded apices; an attached rap...

DEVELOPMENT OF MUCILAGINOUS SURFACES IN EUGLENOIDS. I. STALK MORPHOLOGY OF COLACIUM MUCRONATUM1

The envelope and stalk of Colacium mucronatum Bourr. & Chad, were examined in living cells with light microscopy and in fixed preparations with scanning electron microscopy using critically point dried (CPD) and freeze dried (FD) preparations. The envelope of palmelloid cells is formed over the entire cell surface by many individual strands attached at right angles to areas of articulation of the pellicular strips. Strands were observed to anastomose on the posterior tip of otherwise naked cells. Stalks of living cells in India ink preparations had an optically dark inner core with a lighter outer sheath. In FD stalks a definite inner core was not evident, whereas CPD stalks had an outer surface composed of thick strands which may be the collapsed and aggregated strands of the FD stalks. In both there was also an amorphous matrix. The stalk forms from the aggregation of many strands from the anterior cell tip back to a point encompassing the cell surface anterior to a cross section of the tip 9 μm diam. The outer surface of the stalk comes from the pellicular surface joining that area and the core from the cell tip in the area of the canal opening. Any possible participation of the inner canal surface in stalk formation could not be determined because of the great density of the mucilage at the cell‐tip/stalk junction.

SURFACE CONFIGURATION OF THE LORICA OF THE EUGLENOID TRACHELOMONAS AS REVEALED WITH SCANNING ELECTRON MICROSCOPY

The surface of Trachelomonas was examined readily with SEM at magnifications up to X 20,000 in unfixed or fixed material. Cells were placed directly on specimen holders without washing, air dried, and coated with aluminum or gold. Clones of T. grandis, T. hispida var. coronata, and T. oblonga var. punctata and three species from a natural collection showed the following features: the lorica was punctate or solid, and the surface projections, when present, consisted of minute papillae (0.1 μm), larger, often globose papillae (up to 0.8 μm), and spines which tapered to a point or which had parallel sides and ended bluntly; spines appeared hollow or solid. Pringsheims clone of T. oblonga var. punctata, which he described as a new spineless variety, possessed short tapering spines and globose papillae. Such observations suggest that a major problem in delimiting species may be in discovering the ornamentation potential of a clone. The discovery of new features of the lorica (e.g., minute papillae and hollow projections), the clarification of shapes of surface features, and, in general, the excellent resolution at 10 times the usable magnification of light microscopy dictate a reexamination of known species with SEM. We suggest that a SEM study of the variation in the lorica surface in clonal material will lead to a recognition of polymorphism and eventually to a clearer understanding of taxonomic entities described from natural collections.

OBSERVATIONS ON THE EUGLENOID COLACIUM WITH SPECIAL REFERENCE TO THE FORMATION AND MORPHOLOGY OF ATTACHMENT MATERIAL1

Certain taxonomic features of Colacium Ehrb. are evaluated from field, clone, and literature studies. A main character, morphology of the attachment material, is shown to be partially nutritionally controlled: stalks and cushion holdfasts are produced in soil‐water but rarely in plain Euglena medium; ferric and manganouns compounds influence the, formation of stalks in C. vesiculosum; single clones of C. vesiculosum produce holdfast characteristics of C. arbuscula, C. steinii, C. sideropus, and C. simplex when grown in soil‐water medium. Stalk formation is rare in C. vesiculosum but common in C. mucronatum and Colacium sp. (from the rectum of damselflies). Some questionable negative observations, incompleteness of certain species descriptions, and overlapping of species characteristics lead us to believe that C. sequabile, C. stentorinum, C. calvum, C. multoculata, C. elongatum, C. ovale, C. arcuatum, C. cyclopicola, and C. pyrenophorum = C. vesiculosum. Our C. vesiculosum attached to Mougeotia and Volvox tertius, suggesting that the epiphytic species of Colacium, C. epiphyticum, and C. parasiticum need to be studied in clonal culture to determine if they have substrate specificity, and if they represent valid species. Recommendations are made for identifying and naming species.

CRYPTOGLENA PIGRA: A EUGLENOID WITH ONE CHLOROPLAST12

The taxonomic status of Cryptoglena pigra Ehrb., interpreted from observations based on bright‐field microscopy, has been uncertain. Examination with the electron microscope of a clone of C pigra isolated by E. G. Pringsheim reveals certain features which, collectively, are distinctly euglenoid: periplast associated with muciferous bodies and subpellicular microtubules; canal and reservoir with microtubules; one flagellum with a swelling and emergent through a canal, and a second flagellum without a swelling and nonremergent; stigma (eyetpot) closely apprrssed to but not part of the chloroplast; nucleus with permanently condensed chromosomes attached to the inner nuclrar membrane; mitochondria with disc‐shaped cristae constricted at the base; chloroplast with thylakoids often in triplets; and paramylon grains in the cytoplasm. Unlike most euglenoids, C. pigra possesses a single chloroplast that in transverse thin sections is U‐shaped.

DEVELOPMENT OF MUCILAGINOUS SURFACES IN EUGLENOIDS. II. FLAGELLATED, CREEPING AND PALMELLOID CELLS OF EUGLENA1

Critical‐point dried (CPD) cells from clonal cultures of Euglena gracilis Klebs (Z strain), E. deses Ehrb., E. tripteris (Duj.) Klebs and E. myxocylindracea Bold & MacEntee were examined by scanning electron microscopy. Flagellated motile cells of E. gracilis are naked except for a few strands of mucilage on the posterior tip. Flagellated cells of E. tripteris have a permanent mucilage coating often of uneven distribution and usually not as well developed as that of nonflagellated creeping cells which have a distinctive mucilage. In E. deses the coating appears rough due to the aggregation of isolated groups of strands above the cell surface. In E. tripteris the coating appears smooth except for breaks near the articulation of the pellicular strips where the mucilage may rise above the surface to form waves. At high magnification this mucilage consists of a network of strands generally lying parallel to the cell surface; the strands become obscure in some specimens. In E. myxocylindracea elongated, mucilage‐coated cells contract to form spheres which undergo further mucilage deposition producing the mucilage covering of palmellae. As palmellae mature, the mucilage surface becomes less porous and the individuality of most mucilage strands is lost.